Ruthenium nanoparticles in high-throughput studies of chemoselective carbonyl hydrogenation reactions
Abstract Small (≤1.4?nm) and very active Ru nanoparticles, stabilized in a polysiloxane matrix, were prepared and studied in hydrogenation reactions by the integration of catalysis and analysis. We used our strategy to combine catalytic activity and separation selectivity in a capillary microreactor...
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| Main Authors: | , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2016
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| In: |
ChemCatChem
Year: 2015, Volume: 8, Issue: 3, Pages: 571-576 |
| ISSN: | 1867-3899 |
| DOI: | 10.1002/cctc.201501069 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/cctc.201501069 Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/cctc.201501069 |
| Author Notes: | Julia Gmeiner, Silke Behrens, Bernd Spliethoff, and Oliver Trapp |
| Summary: | Abstract Small (≤1.4?nm) and very active Ru nanoparticles, stabilized in a polysiloxane matrix, were prepared and studied in hydrogenation reactions by the integration of catalysis and analysis. We used our strategy to combine catalytic activity and separation selectivity in a capillary microreactor, installed in a GC?MS instrument, to develop a fast and reliable screening tool for catalysis over Ru nanoparticles. A high conversion using a low catalyst loading of 0.3?mol?% and temperature and long-term stability of the catalytically active column were observed for the hydrogenation of various carbonyl compounds, which included aldehydes, ketones, and pyruvates. Additionally, we observed a high chemoselectivity for aromatic carbonyl systems. Comprehensive measurements were performed in this high-throughput experimental setup to gain important insights into the kinetics of hydrogenation reactions at the interface between heterogeneous and homogeneous catalysis. |
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| Item Description: | First published: 23 December 2015 Gesehen am 19.06.2020 |
| Physical Description: | Online Resource |
| ISSN: | 1867-3899 |
| DOI: | 10.1002/cctc.201501069 |